From cells to chromatin: Capturing snapshots of genome organization with 5C technology

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• 作者：Maria A. Ferraiuolo^a ; ^{maria.ferraiuolo@mail.mcgill.ca} ; Amartya Sanyal^b ; ^{Amartya.Sanyal@umassmed.edu} ; Natalia Naumova^b ; ^{Natalia.Naumova@umassmed.edu} ; Job Dekker^b ; ^{Job.Dekker@umassmed.edu} ; José ; e Dostie^a ; ^{josee.dostie@mcgill.ca}
• 关键词：Chromatin ; Transcription ; Epigenetics ; Genome architecture ; Structure
• 刊名：Methods
• 出版年：2012
• 出版时间：November, 2012
• 年：2012
• 卷：58
• 期：3
• 页码：255-267
• 全文大小：564 K

文摘

In eukaryotes, genome organization can be observed on many levels and at different scales. This organization is important not only to reduce chromosome length but also for the proper execution of various biological processes. High-resolution mapping of spatial chromatin structure was made possible by the development of the chromosome conformation capture (3C) technique. 3C uses chemical cross-linking followed by proximity-based ligation of fragmented DNA to capture frequently interacting chromatin segments in cell populations. Several 3C-related methods capable of higher chromosome conformation mapping throughput were reported afterwards. These techniques include the 3C-carbon copy (5C) approach, which offers the advantage of being highly quantitative and reproducible. We provide here an updated reference protocol for the production of 5C libraries analyzed by next-generation sequencing or onto microarrays. A procedure used to verify that 3C library templates bear the high quality required to produce superior 5C libraries is also described. We believe that this detailed protocol will help guide researchers in probing spatial genome organization and its role in various biological processes.